FYCO1 Polyclonal Antibody
规格: | / 20μL / 60μL / 120μL / 200μL |
价格: | / ¥420 / ¥1010 / ¥1640 / ¥2365 |
货号:E-AB-19197
宿主: Rabbit
反应性: H
应用: IHC
Overview
Synonyms | CATC2,CTRCT18,DKFZp779K1152,FLJ13335,FYCO1,FYCO1,FYVE and coiled coil domain containing 1,FYVE and coiled coil domain containing protein 1,FYVE and coiled-coil domain-containing protein 1,MGC126517,MGC126519,RUFY3,RUN and FYVE domain containing 3,ZFYVE7,Zinc finger FYVE domain containing protein 7,Zinc finger FYVE domain-containing protein 7,FYCO1抗体 |
Swissprot | Q9BQS8 |
Source | Rabbit |
Reactivity | Human |
Immunogen | Fusion protein of human FYCO1 |
Application | IHC(Detection kit: E-IR-R213) |
Recommended dilution | IHC,,1:100-1:200 |
Concentration | 1.92mg/mL |
Clonality | Polyclonal |
Properties
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 |
Background | This gene encodes a protein that contains a RUN domain, FYVE-type zinc finger domain and Golgi dynamics (GOLD) domain. The encoded protein plays a role in microtubule plus end-directed transport of autophagic vesicles through interactions with the small GTPase Rab7, phosphatidylinositol-3-phosphate (PI3P) and the autophagosome marker LC3. Mutations in this gene are a cause of autosomal recessive congenital cataract-2 (CATC2). |